Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
- Vacancy details:
- Department:Quality Control Associate
- Qualification: Masters’s degree in Biotechnology/ BE Biotechnology/B Tech Biotechnology or in Biochemistry domain.
- Experienced:3 to 6 years
- Salary: ₹Not Disclosed
Job Description: Greetings from Dr. Reddy’s Laboratories Limited.!!
- Important Details :
- Location: Hyderabad
- Post of date:09/08/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Description
Job Summary
We are seeking an associate for the Quality control -Analytical team responsible for conducting analysis of Biosimilar products ( drug substance , drug products and their inprocess samples). The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.
” Roles & Responsibilities
To perform analysis in Quality control analytical laboratory for the Biosimilar /Biologics Products as per the planning allotted by Team lead
To perform Gel electrophoresis/CZE/HCP/HCD analysis of Biosimilar Molecules
Having 3 to 6 years of experience
Method Validations on HCP/HCD/CZE/SDS PAGE
To Perform Biochemical, Physico chemical and chromatographic analysis
Adhering to GMP practices
Adhering to Good documentation practices
Adhering to Good Analytical Practices
Adhering to Regulatory Requirements including Internal or External audits, Audit readiness and Query response drafting.
Adhering to compliance of systems in Quality Control, by working with relevant stake holders
To adhere and follow the safety practices and procedures.
To adhere to various cGMP procedures and internal SOPs
Qualifications
Educational qualification:
A Masters’s degree in Biotechnology/ BE Biotechnology/B Tech Biotechnology or in Biochemistry domain.
Minimum work experience:
3 to 6 years of experience in QC analytical testing in Biosimilar products
Skills & attributes: Technical Skills
Proficient in handling SEC/RP/IEX/Peptide Mapping/Glycan analysis of Biosimilar Products
Proficient in handling of Gel electrophoresis/CE/HCP/HCD analysis of Biosimilar products
Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications.
Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment).
Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents.
Method Validations on HCP/HCD/CZE/SDS PAGE
Behavioural Skills
Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks.
Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates.
Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities.
Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations.
Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities.
Additional Information
” Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions…
For more details, please visit our career website at https://careers.drreddys.com/#!/
